Golf Ball and Thermoplastic Material

ABSTRACT

Disclosed herein is novel thermoplastic material and a golf ball utilizing the thermoplastic material of the invention. The golf ball ( 10 ) preferably comprises a core ( 12 ), a cover ( 16 ) and, optionally, a boundary layer ( 14 ). At least one of the core ( 12 ), cover ( 16 ) or boundary layer ( 14 ) of the golf ball ( 10 ) comprises a thermoplastic material according to the invention. The thermoplastic material comprises a partially to highly neutralized blend of acid and alkyl acrylate copolymers, which additionally comprise a fatty acid or fatty acid salt. A golf ball comprising a component that incorporates the thermoplastic material of the invention has a soft feel and resilience that is maintained or improved compared to a standard golf ball.

CROSS REFERENCES TO RELATED APPLICATIONS

The Present Application is a continuation of U.S. patent applicationSer. No. 11/276,199 filed on Feb. 17, 2006, which is acontinuation-in-part application of U.S. patent application Ser. No.10/905,925, filed on Jan. 26, 2005, now U.S. Pat. No. 7,156,755.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a thermoplastic material and to its usein a golf ball.

2. Description of the Related Art

Traditional golf ball covers have been comprised of balata or blends ofbalata with elastomeric or plastic materials. Balata-related covers,often referred to as soft balata covers, are relatively soft andflexible. Upon impact, soft balata covers compress against the surfaceof the club producing high spin. Consequently, these soft and flexiblecovers provide an experienced golfer with the ability to apply a spin tocontrol the ball in flight in order to produce a draw or a fade, or abackspin which causes the ball to “bite” or stop abruptly on contactwith the green. Moreover, soft balata covers produce a soft “feel” tothe low handicap player. Such playability properties as, workability andfeel are particularly important in short iron play with low swing speedsand are exploited significantly by relatively skilled players.

Despite all the benefits of balata, balata-related golf ball covers areeasily cut and/or damaged if hit improperly. Golf balls produced withbalata or balata-containing cover compositions therefore have arelatively short lifespan. As a result of this negative property, balataand its synthetic substitutes, trans-polybutadiene andtrans-polyisoprene, have been essentially replaced as the covermaterials of choice by new cover materials comprising ionomeric resins.

Ionomeric resins are polymers containing interchain ionic bonding. As aresult of their toughness, durability and flight characteristics,various ionomeric resins sold by E.I. du Pont de Nemours and Company(DuPont), under the trade name “Surlyn7” (Surlyn7™), and, more recently,by the ExxonMobil Corporation (ExxonMobil) (see, for example, U.S. Pat.No. 4,911,451), under the trade name “Iotek” (Iotek™), have become thematerials of choice for the construction of golf ball covers overtraditional balata (trans-polyisoprene, natural or synthetic) rubbers.

Ionomeric resins are generally ionic copolymers of an olefin (such asethylene) and a metal salt of an unsaturated carboxylic acid (such asacrylic acid, methacrylic acid or maleic acid). Metal cations such assodium or zinc are used to neutralize some portion of the acidic groupin the copolymer resulting in a thermoplastic elastomer exhibitingenhanced properties such as durability for golf ball cover constructionover balata. However, some of the advantages gained in increaseddurability have been offset to some degree by decreases produced inplayability. This is because although ionomeric resins are very durable,they tend to be very hard when utilized for golf ball cover constructionand, thus, lack the degree of softness required to impart the spinnecessary to control the ball in flight. Since the ionomeric resins areharder than balata, the ionomeric resin covers do not compress as muchagainst the face of the club upon impact, thereby producing less spin.In addition, the harder and more durable ionomeric resins lack the feelcharacteristic associated with the softer balata-related covers.

As a result, while there are many commercial grades of ionomersavailable both from DuPont and ExxonMobil, with a wide range ofproperties that vary according to the type and amount of metal cations,molecular weight, composition of the base resin (such as relativecontent of ethylene and methacrylic and/or acrylic acid groups) andadditive ingredients such as reinforcement agents, or the like, a greatdeal of research continues in order to develop a golf ball covercomposition exhibiting not only the improved impact resistance andcarrying distance properties produced by the “hard” ionomeric resins,but also the playability (for example, “spin”, “feel” and the like)characteristics previously associated with soft balata-related covers,properties that are still desired by the more skilled golfer.

Consequently, a number of golf balls have been produced to address theseneeds. The different types of materials utilized to formulate the cores,mantles and covers of these balls dramatically alter the balls' overallcharacteristics. In addition, multi-layered covers containing one ormore ionomeric resins have also been formulated in an attempt to producea golf ball having the overall distance, playability and durabilitycharacteristics desired.

Such formulations are described in U.S. Pat. No. 4,431,193 ('193), wherea multi-layered golf ball is produced by initially molding a first coverlayer on a spherical core and then adding a second layer. The firstlayer consists of a hard, high flexural modulus resinous material suchas Surlyn7™ 8940, a sodium ion based low acid (less than or equal to 16weight percent methacrylic acid) ionomeric resin having a flexuralmodulus of about 51,000 psi. An outer layer of a comparatively soft, lowflexural modulus resinous material such Surlyn7™ 9020 is molded over theinner cover layer. Surlyn7™ 9020 is a zinc ion based low acid (10 weightpercent methacrylic acid) ionomeric resin having a flexural modulus ofabout 14,000 psi.

The '193 patent also teaches that the hard, high flexural modulus resin,which comprises the first layer, provides for a gain in coefficient ofrestitution over the coefficient of restitution of the core. Theincrease in the coefficient of restitution provides a ball that attainsor approaches the maximum initial velocity limit of 255 feet per second,as provided by the United States Golf Association (USGA) rules. Therelatively soft, low flexural modulus outer layer provides for theadvantageous feel and playing characteristics of a balata covered golfball.

In various attempts to produce a durable, high spin golf ball, thegolfing industry has blended the hard ionomeric resins with a number ofsofter ionomeric resins. For example, U.S. Pat. Nos. 4,884,814 and5,120,791 are directed to cover compositions containing blends of hardand soft ionomeric resins. The hard copolymers typically are made froman olefin and an unsaturated carboxylic acid. The soft copolymers aregenerally made from an olefin, an unsaturated carboxylic acid and anacrylate ester. However, it has been found that golf ball covers formedfrom hard-soft ionomer blends tend to become scuffed more readily thancovers made of a hard ionomeric resin alone. It would be useful todevelop a golf ball having a combination of softness and durability thatis better than the softness-durability combination of a golf ball covermade from a hard-soft ionomer blend.

Most professional golfers and good amateur golfers desire a golf ballthat provides distance when hit off a driver, control and stoppingability on full iron shots as well as high spin on short “touch andfeel” shots. Many conventional golf balls have undesirable high spinrates on full shots. The excessive spin on full shots is a sacrificemade in order to achieve more spin on the shorter touch shots. It wouldbe beneficial to provide a golf ball that has high spin for touch shots,without generating excessive spin on full shots, while maintaining orimproving some of the other properties of the golf ball.

BRIEF SUMMARY OF THE INVENTION

The present invention is directed to a novel thermoplastic material andto its use in a golf ball as a core, cover or intermediate layer. Thethermoplastic material of the invention includes a blend of two or morecopolymers and fatty acids or salts of fatty acids. The material of theinvention is partially to highly neutralized (preferably 50 to 100%),and has a greater coefficient of restitution than other thermoplasticmaterials.

One embodiment of the present invention is a golf ball comprising a coreand a cover layer disposed on and, preferably, covering the core,wherein at least one of the cover and the core is formed from thethermoplastic material of the invention. The thermoplastic material ofthe invention preferably comprises, as part of the blend, (1) acopolymer comprising an alpha olefin and an acid, such asethylene/acrylic acid (an alpha, beta-unsaturated carboxylic acid), and(2) a copolymer of an alpha olefin and an alkyl acrylate, such asethylene/butyl acrylate. Alternatively, the first copolymer may includean alpha olefin, an acid and a softening comonomer such as an alkylacrylate (wherein the first copolymer is also referred to as aterpolymer). A thermoplastic material blend of the invention furthercomprises fatty acids or fatty acid salts. Exemplary fatty acids orfatty acid salts can include metal stearates or stearic acids. Othermaterials such as metallocene-catalyzed plastomers, urethanes or othermaterials known in the art may also be used for thermoplastic materialblend modification as desired.

In a particularly preferred form of the invention the thermoplasticmaterial of the invention comprises a blend of two or more copolymers,wherein the first copolymer is formed from an alpha olefin having 2 to 8carbon atoms, and an acid which includes at least one member selectedfrom the group consisting of alpha, beta-ethylenically unsaturated mono-or dicarboxylic acids with a portion of the acid being neutralized withcations, and the second copolymer is formed from an alpha olefin having2 to 8 carbon atoms, and an alkyl acrylate having from 1 to 8 carbonatoms in the alkyl group. The optional softening comonomer that may beadded to the first copolymer is, preferably, an unsaturated monomer ofthe acrylate ester class having from 1 to 21 carbon atoms.

Another embodiment of the present invention is a golf ball having acore, boundary layer and cover. The core includes a polybutadienemixture, has a diameter ranging from 1.35 inches to 1.64 inches and hasa PGA compression ranging from 50 to 90. The boundary layer is formedover the core and is composed of a thermoplastic material of theinvention. The boundary layer has a thickness ranging from 0.020 to0.075 inches and a Shore D hardness ranging from 50 to 70 as measuredaccording to standard test method D2240 of the American Society forTesting and Materials (ASTM-D2240). The cover is formed over theboundary layer. The cover is composed of a fast chemical reactionaliphatic polyurethane material formed from reactants that comprise apolyurethane prepolymer and a polyol. The polyurethane material has aShore D hardness ranging from 30 to 60 as measured according toASTM-D2240 and a thickness ranging from 0.015 to 0.044 inches. Thepolyurethane material of the cover also provides for an aerodynamicsurface geometry.

Having briefly described the present invention, the above and furtherobjects, features and advantages thereof will be recognized by thoseskilled in the pertinent art from the following detailed description ofthe invention when taken in conjunction with the accompanying drawings.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

FIG. 1 illustrates a perspective view of a golf ball of the presentinvention including a cut-away portion showing a core, a boundary layerand a cover.

FIG. 2 illustrates a perspective view of a golf ball of the presentinvention including a cut-away portion showing a core and a cover.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a novel thermoplastic material and toits use in golf equipment, particularly, a golf ball 10. As shown inFIG. 1, a three-piece solid golf ball comprises a core 12, a boundary 14and a cover 16. As shown in FIG. 2, a two-piece golf ball comprises acore 12 and a cover 16. At least one of the components of the golf ballcomprises a thermoplastic material of the invention.

More particularly, the invention provides a neutralized thermoplasticmaterial comprising a blend of (1) a copolymer comprising an alphaolefin and an alpha, beta-unsaturated carboxylic acid (an acid copolymerreferred to as EX), (2) a copolymer of an alpha olefin and an alkylacrylate (an alkyl acrylate copolymer referred to as EY) and 3) a fattyacid or salt of a fatty acid. The first copolymer may also include asoftening comonomer such as an alkyl acrylate, which copolymer (orterpolymer) is referred to as EXY. Other materials, including but notlimited to, urethanes and the like maybe used to modify the blend Theacid copolymer of a thermoplastic material of the invention may containanywhere from 1 to 30% by weight acid. A high acid copolymer containinggreater than 16% by weight acid, preferably, from about 17 to about 25weight % acid and, more preferably, about 20 weight % acid, or a lowacid copolymer containing 16% byweight acid or less maybe used asdesired. The acid copolymer is neutralized with a metal cation of a salt(a metal cation salt) capable of ionizing or neutralizing the copolymerto the extent desired, generally from about 10 to 100%, preferably, from30 to 100% and, more preferably, from 40 to 90%. The amount of metalcation salt needed varies with the extent of neutralization desired.

The acid copolymer is preferably made up of from about 10 to about 30%by weight of an alpha, beta-unsaturated carboxylic acid and an alphaolefin. Optionally, a softening comonomer can be included in thecopolymer. Generally, the alpha olefin has from 2 to 10 carbon atoms andis, preferably, ethylene. The unsaturated carboxylic acid is an acidhaving from about 3 to 8 carbon atoms. Examples of such acids include,but are not limited to, acrylic acid, methacrylic acid, ethacrylic acid,chloroacrylic acid, crotonic acid, maleic acid, fumaric acid anditaconic acid, with acrylic acid and methacrylic acid being preferred.The optional softening comonomer, such as an alkyl acrylate, has, e.g.,from 1 to 8 carbon atoms in the alkyl group. The acid copolymer broadlycontains from 1 to about 30% by weight unsaturated carboxylic acid, fromabout 70 to about 99% by weight ethylene and from 0 to about 40% byweight of a softening comonomer.

Examples of acid copolymers suitable for use in a thermoplastic materialof the invention include, but are not limited to, an ethylene/acrylicacid copolymer, an ethylene/methacrylic acid copolymer, anethylene/itaconic acid copolymer, an ethylene/maleic acid copolymer, anethylene/methacrylic acid/alkyl acrylate terpolymer, or anethylene/acrylic acid/alkyl acrylate terpolymer.

Acid copolymers are well known in the golf ball art. Examples of acidcopolymers that fulfill the criteria set forth above include, but arenot limited to, those sold under the trade names Escor™(ethylene/acrylic acid copolymers) and Iotek™ (ethylene/acrylicacid/acrylate terpolymers) by ExxonMobil, namely, Escor™ 959, Escor™960, Escor™ AT325 and Iotek™ 7510. Other examples of acid copolymersinclude those sold under the trade name Primacor™ (ethylene/acrylic acidcopolymers) by Dow Chemical Company, namely Primacor™ 5980I andPrimacor™ 3340I. Other acid copolymers that may be used includeethylene/methacrylic acid copolymers such as sold under the trade namesSurlyn™ and Nucrel™ by DuPont. Surlyn™ copolymers are neutralized withzinc, sodium or lithium ions. Nucrel™ copolymers are inherently flexiblelike ethylene vinyl acetate (EVA) copolymers and offer desirableperformance characteristics similar to those of Surlyn™. Nucrel™copolymers are produced by reacting ethylene and methacrylic acid in thepresence of free radical initiators. A branched, randomethylene/methacrylic acid (EMAA) copolymer is produced thereby. Carboxylgroups are distributed along the polymer chain and interact withcarboxyl groups on adjacent molecules to form a weakly cross-linkednetwork through hydrogen bonding. Nucrel™ and Surlyn™ terpolymers arealso available for use in a thermoplastic material of the invention.

Acid copolymers of a thermoplastic material of the invention areneutralized to a desired percentage through the use of metal cationsalts. The salts utilized are those that provide the metal cationscapable of neutralizing, to various extents, the carboxylic acid groupsof the acid copolymer. These salts include, for example, acetate, oxideor hydroxide salts of lithium, calcium, zinc, sodium, potassium, nickel,magnesium, aluminum, zirconium or manganese.

Some examples of salts comprising lithium cations are lithium hydroxidemonohydrate, lithium hydroxide, lithium oxide and lithium acetate. Saltscomprising calcium cations include calcium hydroxide, calcium acetateand calcium oxide. Suitable salts comprising zinc cations are zincacetate dihydrate, zinc acetate or a blend of zinc oxide and aceticacid. Examples of salts comprising sodium cations include sodiumhydroxide and sodium acetate. Similarly, salts comprising potassiumcations include potassium hydroxide and potassium acetate. Suitablesalts comprising nickel cations are nickel acetate, nickel oxide andnickel hydroxide. Salts comprising magnesium cations include magnesiumoxide, magnesium hydroxide and magnesium acetate. Salts comprisingmanganese cations include manganese acetate and manganese oxide.

Additionally a wide variety of pre-neutralized acid polymers arecommercially available for a thermoplastic material of the invention.These pre-neutralized acid polymers include both hard and softpre-neutralized ionomeric resins as well as both low and high acidpre-neutralized ionomeric resins.

Hard (high modulus) pre-neutralized ionomeric resins include thosehaving a hardness greater than 50 on the Shore D scale as measured inaccordance with ASTM D-2240 and a flexural modulus from about 15,000 toabout 70,000 psi as measured in accordance with ASTM standard testmethod D-790 (ASTM D-790).

Soft (low modulus) pre-neutralized ionomeric resins are generallyacrylic acid or methacrylic acid based. One example of a softpre-neutralized ionomer resin comprises a zinc based ionomer made froman acrylic acid polymer and unsaturated monomers of the acrylate esterclass. The soft ionomeric resins generally have a hardness from about 20to about 50 or, preferably, from about 30 to about 40 as measured on theShore D scale and a flexural modulus from about 2,000 to about 15,000psi or, preferably, from about 3,000 to 10,000 psi as measured inaccordance with ASTM D-790. Examples of hard and soft ionomeric resinsinclude those sold under the Iotek™ and Surlyn™ trade names.

The golf ball 10 has at least one layer composed of the thermoplasticmaterial of the invention comprising about 10 to about 95% by weight ofat least one neutralized acid copolymer and, preferably, from about 15to about 90% acid copolymer.

Generally, ethylene/alkyl acrylate copolymers include ethylene andacrylic or methacrylic esters of linear, branched or cyclic alkanols.Preferably, the copolymers contain from about 1 to about 35 weight %alkyl acrylate and from about 99 to about 65 weight % ethylene.

Examples of ethylene/alkyl acrylate copolymers that may be used include,among others, ethylene/ethyl acrylate (EEA), ethylene/methyl acrylate(EMA) and ethylene/butyl acrylate (EBA). EEA copolymers are made by thepolymerization of ethylene units with randomly distributed ethyleneacrylate (EA) monomer groups. The copolymers contain up to about 30% byweight of EA. The copolymers are tough and flexible having a relativelyhigh molecular weight. The copolymers have good flexural fatigue and lowtemperature properties (down to −65° C.). In addition, EEA resistsenvironmental stress cracking as well as ultraviolet (UV) radiation.Examples of EEA copolymers include those sold under the trade nameBakelite™ by the Union Carbide Corporation. EEA is similar to ethylenevinyl acetate (EVA) in its density-property relationships andhigh-temperature resistance. In addition, like EVA, EEA is not resistantto aliphatic and aromatic hydrocarbons.

EMA copolymers contain up to about 30% by weight of methyl acrylate andyield blown films having rubberlike limpness and high impact strength.These copolymers may be useful in coating and laminating applications asa result of their good adhesion to commonly used substrates. EMA alsohas good heat-seal characteristics.

EMA copolymers are manufactured by reacting, at high temperatures andpressures, methyl acrylate monomers with ethylene and free radicalinitiators. Polymerization occurs such that the methyl acrylate formsrandom pendant groups on the polyethylene backbone. The acrylicfunctionality decreases polymer crystallinity and increases polarity,enhancing polymer properties. These properties depend on molecularweight (determined, for example, by melt index) and percentcrystallinity. Percent crystallinity is determined by the extent ofmethyl acrylate comonomer incorporation. As the methyl acrylate contentincreases, the film becomes softer, tougher and easier to heat seal.

EMA films have low moduli (generally less than 10,000 psi), low meltingpoints and good impact strengths. In addition, EMA copolymers are highlypolar and, as a result, are compatible with olefinic and other polymers.They adhere well to many substrates including low density polyethylene(LDPE), linear low density polyethylene (LLDPE) and EVA.

Examples of EMA copolymers for use in the golf ball components of thepresent invention include those sold under the trade names Optema™ orEscor™ by ExxonMobil . Optema™ and Escor™ are thermally stable polymersthat will accept up to 65% or more fillers and pigments without losingtheir properties. These copolymers are more thermally stable than EVAand can be extruded or molded over a range of temperatures from 275 to625° F. (compared to the limit of 450° F. for EVA copolymers). EMAcopolymers are generally not corrosive as compared to EVA and EAAcopolymers.

EBA copolymers can also be included in a thermoplastic material of theinvention. These are generally similar to EMA copolymers with improvedlow temperature impact strength and high clarity. For example, the EBAcopolymer sold under the trade name EBAC™ by the Chevron Corporation isstable at high temperatures and may be processed as high as 600° F.Metal cation salts may also be utilized to neutralize ethylene/alkylacrylate copolymers as a source of the corresponding carboxylic acid.The salts to be used are those salts that provide the metal cationscapable of hydrolyzing and neutralizing, to various extents, thecarboxylic acid ester groups of the copolymers. This converts the alkylester into a metal salt of the acid. These metal cation salts include,but are not limited to, oxide, carbonate or hydroxide salts of alkalimetals such as lithium, sodium, potassium or mixtures thereof. Someexamples hydroxide salts of alkali metals include, but are not limitedto, lithium hydroxide monohydrate, lithium hydroxide, lithium carbonate,lithium oxide, sodium hydroxide, sodium oxide, sodium carbonate,potassium hydroxide, potassium oxide and potassium carbonate.

The amount of metal cation salt, preferably, an alkali metal cation saltreacted with an ethylene/alkyl acrylate copolymer varies depending uponsuch factors as the reactivity of the salt and copolymer used, reactionconditions (such as temperature, pressure, moisture content and thelike) and the desired level of conversion. Preferably, the reactionoccurs through saponification, wherein the carboxylic acid ester groupsof the ethylene/alkyl acrylate copolymer are converted by alkalinehydrolysis to form the salt of the acid and alcohol. Examples of suchreactions are set forth in U.S. Pat. Nos. 3,970,626, 4,638,034 and5,218,057, which are incorporated herein by reference.

The products of the conversion reaction are an alkanol (the alkyl groupof which comes from the alkyl acrylate comonomer) and a terpolymer ofethylene, alkyl acrylate, and an alkali metal salt of the (meth)acrylicacid. The degree of conversion or saponification is variable dependingon the amount of alkali metal cation salt used and the saponificationconditions. Generally, from about 10 to about 60% of the ester groupsare converted during the saponification reaction. The alkanol and otherby products can be removed by normal separation processes leaving theremaining metal cation neutralized (or hydrolyzed) ester-based ionomerresin reaction product.

Alternatively, the ethylene alkyl acrylate copolymer included in theinvention can be commercially obtained in a pre-neutralized orsaponified condition. For example, a number of metal cation neutralizedester-based ionomer resins produced under the saponification process ofU.S. Pat. No. 5,218,057 are available from the Chevron Corporation.

Additional examples of the preferred copolymers that fulfill thecriteria set forth above are a series of acrylate copolymers that arecommercially available from ExxonMobil, such as Optema™ ethylene methylacrylates and Enable™ ethylene butyl acrylates; Elvaloy™ ethylene butylacrylates available from DuPont, and Lotryl™ ethylene butyl acrylicesters available from Atofina Chemical.

The acrylate ester is preferably an unsaturated monomer having from 1 to21 carbon atoms, which serves as a softening comonomer. The acrylateester preferably is methyl, ethyl, n-propyl, n-butyl, n-octyl,2-ethylhexyl or 2-methoxyethyl 1-acrylate and most preferably is methylacrylate or n-butyl acrylate. Another suitable type of softeningcomonomer is an alkyl vinyl ether selected from the group consisting ofn-butyl, n-hexyl, 2-ethylhexyl and 2-methoxyethyl vinyl ethers.

The acrylate ester-containing ionic copolymer or copolymers used in golfball components can be obtained by neutralizing commercially availableacrylate ester-containing acid copolymers such as poly (ethylene/methylacrylate/acrylic acid) terpolymers sold by ExxonMobil under the tradename Escor™ ATX or poly (ethylene/butyl acrylate/methacrylic acid)terpolymers sold by DuPont under the trade name Nucrel™. The acid groupsof these materials and blends thereof are neutralized with one or moreof various metal cation salts that include zinc, sodium, magnesium,lithium, potassium, calcium, manganese, nickel and the like. The extentof neutralization can range from 10 to about 100%, preferably from about30 to about 100% or, more preferably, from about 40 to about 90%.Generally, a higher degree of neutralization results in a harder andtougher thermoplastic material.

The fatty acids and salts of fatty acids generally comprise fatty acidsneutralized with metal cations. The fatty acids can be saturated orunsaturated fatty acids and are generally composed of a chain of alkylgroups containing from about 2 to about 80 carbon atoms, preferably fromabout 4 to about 30, usually an even number, and terminate with acarboxyl (—COOH) group. The general formula for fatty acids (except foracetic acid) is CH₃(CH₂)_(X)COOH, wherein the carbon atom count includesthe carboxyl group and X is from about 4 to about 30 carbon atoms.Examples of fatty acids suitable for use include, but are not limitedto, stearic acid, oleic acid, palmitic acid, pelargonic acid, lauricacid, butyric acid, valeric acid, caproic acid, caprylic acid, capricacid, myristic acid, margaric acid, arachidic acid, behenic acid,lignoceric acid, cerotic acid, carboceric acid, montanic acid andmelissic acid. Such fatty acids are preferably neutralized with metalcations such as zinc, calcium, magnesium, barium, sodium, lithium,aluminum or combinations thereof, although other metal cations may alsobe used. The metal cations are generally from metal cation salts thatneutralize, to various extents, the carboxylic acid groups of the fattyacids. Examples of metal cation salts include sulfate, carbonate,acetate and hydroxylate salts of metals such as zinc, calcium, magnesiumand barium. Examples of the fatty acid salts that may be utilized in athermoplastic material of the invention include, but are not limited to,metal stearates, laureates, oleates, palmitates, pelargonates and thelike such as zinc stearate, calcium stearate, magnesium stearate, bariumstearate and so forth. Metal stearates are known in the art and arecommercially available from various manufacturers.

Highly neutralized blends of copolymers used to form the golf ballcomponents of the present invention can be produced by reacting the twocopolymers with various amounts of the metal cation salts at atemperature above the crystalline melting point of the copolymers, forexample, from about 200 to about 500° F. and, preferably, from about 250to about 425° F. under high shear conditions at a pressures of fromabout 100 to 10,000 psi. Other well known blending techniques in the artmay also be used. The amount of metal cation salt used to produce thehighly neutralized blend of copolymers is the quantity that provides asufficient amount of the metal cations to neutralize a desiredpercentage of the carboxylic acid groups of the acid copolymer. Thecopolymers can be blended before or after neutralization, or they can bemixed and neutralized at the same time (that is, the copolymers, metalcation salts and fatty acids or salts of fatty acids are mixedtogether). The fatty acids or salts of fatty acids are added in thedesired amounts, generally from about 5 to about 100 parts by weight,preferably from about 10 to about 60 parts by weight, more preferablyfrom about 20 to about 50 parts by weight and even more preferably fromabout 30 to about 40 parts by weight.

The various compositions of the present invention may be producedaccording to conventional melt blending procedures. In a preferredembodiment, the copolymers are blended in a Banbury™ type mixer,two-roll mill or extruder prior to neutralization. After blending,neutralization then occurs as the polymers are in a melt or molten statewithin the Banbury™ type mixer, two-roll mill or extruder. The blendedcomposition is then formed into slabs, pellets or the like andmaintained in such a state until molding is desired. Alternatively, asimple dry blend of the pelletized or granulated copolymers, which havepreviously been neutralized to a desired extent (and coloredmasterbatch, if desired) may be prepared and fed directly into theinjection molding machine where homogenization occurs in the mixingsection of the barrel prior to injection into the mold. If necessary,further additives such as inorganic fillers may be added and uniformlymixed in before initiation of the molding process.

The compatibility of a metallocene-catalyzed copolymer with an acidcopolymer results in a thermoplastic material blend having superiorproperties over standard ionomeric resin blends as shown by the resultsprovided in the Examples detailed below.

Additional materials may also be added to a thermoplastic material ofthe invention when utilized for golf equipment so long as such materialsdo not substantially reduce the playability properties of the equipment.Exemplary materials include dyes such as Ultramarine Blue™ sold byWhitaker, Clark & Daniels, Incorporated (see U.S. Pat. No. 4,679,795),pigments such as titanium dioxide, zinc oxide, barium sulfate and zincsulfate, UV absorbers, antioxidants, antistatic agents, and stabilizers.Moreover, the ball cover compositions utilizing the thermoplasticmaterial of the invention may also contain softening agents such asthose disclosed in U.S. Pat. Nos. 5,312,857 and 5,306,760. Exemplarysofteners include plasticizers, processing acids, and the like, andreinforcing materials such as glass fibers and inorganic fillers, aslong as the desired properties of the golf ball produced are notimpaired.

Various fillers may be added to golf ball compositions to reducemanufacturing costs, to increase or decrease weight, to reinforce thethermoplastic material, adjust ball layer density or flex modulus, aidin ball mold release and/or adjust the melt flow index of thethermoplastic material and the like. Examples of heavy weight fillersinclude titanium, tungsten, aluminum, bismuth, nickel, molybdenum, iron,steel, lead, copper, brass, boron, boron carbide whiskers, bronze,cobalt, beryllium, zinc, tin, metal oxides (such as zinc oxide, ironoxide, aluminum oxide, titanium oxide, magnesium oxide, zirconium oxide)and metal stearates (such as zinc stearate, calcium stearate, bariumstearate, lithium stearate and magnesium stearate). Other preferredfillers include limestone (ground calcium or magnesium carbonate) andground flash filler.

Fillers that may be used in the layers of a golf ball (other than theouter cover layer) are typically in a finely divided form such as, forexample, in a particle size generally less than about 20 U.S. standardmesh and, preferably, less than about 100 U.S. standard mesh (except forfibers and flock, which are generally elongated). Flock and fiber sizesshould be small enough to facilitate processing. Filler particle sizewill depend upon the desired effect, cost, ease of addition and dustingconsiderations. A filler for a golf ball layer preferably is selectedfrom the group consisting of precipitated hydrated silica, clay, talc,asbestos, glass fibers, aramid fibers, mica, calcium metasilicate,barium sulfate, zinc sulfide, lithopone, silicates, silicon carbide,diatomaceous earth, polyvinyl chloride, carbonates, metals, metalalloys, tungsten carbide, metal oxides, metal stearates, particulatecarbonaceous materials, micro-balloons and combinations thereof.Non-limiting examples of suitable fillers, their densities or specificgravities (spec. grav.) and preferred uses are listed in Table 1: TABLE1 FILLERS FILLER TYPE SPEC. GRAV. COMMENT Precipitated hydrated silica2.00 1, 2 Clay 2.62 1, 2 Talc 2.85 1, 2 Asbestos 2.50 1, 2 Glass fibers2.55 1, 2 Aramid fibers (KEVLAR) 1.44 1, 2 Mica 2.80 1, 2 Calciummetasilicate 2.90 1, 2 Barium sulfate 4.60 1, 2 Zinc sulfide 4.10 1, 2Lithopone 4.2-4.3 1, 2 Silicates 2.10 1, 2 Silicon carbide platelets3.18 1, 2 Silicon carbide whiskers 3.20 1, 2 Tungsten carbide 15.60  1Diatomaceous earth 2.30 1, 2 Polyvinyl chloride 1.41 1, 2 CARBONATESCalcium carbonate 2.71 1, 2 Magnesium carbonate 2.20 1, 2 METAL ANDALLOYS (POWDERS) Titanium 4.51 1 Tungsten 19.35  1 Aluminum 2.70 1Bismuth 9.78 1 Nickel 8.90 1 Molybdenum 10.20  1 Iron 7.86 1 Steel7.8-7.9 1 Lead 11.40 1, 2 Copper 8.94 1 Brass 8.2-8.4 1 Boron 2.34 1Boron carbide whiskers 2.52 1, 2 Bronze 8.70-8.74 1 Cobalt 8.92 1Beryllium 1.84 1 Zinc 7.14 1 Tin 7.31 1 METAL OXIDES Zinc oxide 5.57 1,2 Iron oxide 5.10 1, 2 Aluminum oxide 4.00 Titanium oxide 3.9-4.1 1, 2Magnesium oxide 3.3-3.5 1, 2 Zirconium oxide 5.73 1, 2 METAL STEARATESZinc stearate 1.09 3, 4 Calcium stearate 1.03 3, 4 Barium stearate 1.233, 4 Lithium stearate 1.01 3, 4 Magnesium stearate 1.03 3, 4 PARTICULATECARBONACEOUS Graphite 1.5-1.8 1, 2 Carbon black 1.80 1, 2 Naturalbitumen 1.2-1.4 1, 2 Cotton flock 1.3-1.4 1, 2 Cellulose flock 1.15-1.5 1, 2 Leather fiber 1.2-1.4 1, 2 MICRO BALLOONS Glass 0.15-1.1  1, 2Ceramic 0.2-0.7 1, 2 Fly ash 0.6-0.8 1, 2 COUPLING AGENTS Titanates0.95-1.17 Zirconates 0.92-1.11 Silane 0.95-1.2 Comments:1. Particularly useful for adjusting density of the cover layer.2. Particularly useful for adjusting flex modulus of the cover layer.3. Particularly useful for adjusting mold release of the cover layer.4. Particularly useful for increasing melt flow index of the coverlayer.

Most fillers except for metal stearates would be expected to reduce themelt flow index of an injection molded golf ball cover layer.

The amount of filler used in a golf ball layer is primarily a functionof the weight and distribution requirements of the ball.

Fillers maybe added to any or all layers of a golf ball. Such fillersmaybe used to adjust the properties of a golf ball layer, reinforce thelayer or for any other purpose. In a thermoplastic material blend of theinvention, reinforcing fillers may be used without detracting from orsignificantly reducing the coefficient of restitution (COR) of thematerial in a golf ball layer.

Together, the core 12 of the golf ball (and any optional core layers)and its cover layer 16 or layers 14 preferably combine to form a ballhaving a diameter of 1.680 inches or more, the minimum diameterpermitted by the rules of the USGA, and weighing no more than 1.62ounces for a regulation golf ball. Oversize golf balls may also beproduced, if desired, using a thermoplastic material blend of theinvention.

In another embodiment of the invention, the golf ball may be a one-pieceor unitary construction golf ball comprising the blend of the invention.A thermoplastic material blend of the invention provides for a verydurable golf ball. Such a golf ball may be painted or may have a clearcoat or other markings if desired.

In a particularly preferred embodiment of the invention, the golf ballhas a dimple pattern that provides coverage of 65% or more. The golfball typically is coated with a durable, abrasion-resistant andrelatively non-yellowing finish coat.

A golf ball and its components can be produced by molding processes thatinclude, but are not limited to, those that are well known in the art.For example, golf ball components can be produced by injection molding,reaction injection molding, liquid injection and/or compression moldingthe partially to highly neutralized thermoplastic material blend of theinvention as a golf ball core, core layer, cover layer and so forth. Oneor more layers of a golf ball may comprise the partially to highlyneutralized blend according to the invention. Other layers of a golfball may be made of the same or different materials and may comprise anysuitable material or blend thereof known in the art.

The thermoplastic material of the invention preferably has a Shore Dhardness of from about 30 to about 80 Shore D as desired. Additionally,a golf ball core, intermediate ball or finished ball may have a PGAcompression of from about 0 to about 160.

After a golf ball has been molded, it may undergo various furtherprocessing steps such as buffing, painting and marking as disclosed inU.S. Pat. No. 4,911,451.

The present invention is further illustrated by the following examplesin which the parts of the specific ingredients are by weight. It is tobe understood that the present invention is not limited to the examplesas various changes and modifications may be made to the inventionwithout departing from the spirit and scope thereof.

EXAMPLES Example 1

Three different highly neutralized blends of olefin/acid/acrylateterpolymers and olefin/acrylate copolymers containing metal stearateswere produced and formed into neat spheres. The neat spheres were testedfor compression and coefficient of restitution. The terpolymer was anethylene/acrylic acid/methyl acrylate terpolymer, and the copolymer wasan ethylene/butyl acrylate copolymer. The terpolymer was used alone andin a blend with the copolymer. A terpolymer control with no metalstearate added was also produced. Each of the blends was neutralized to100% using Mg(OH)₂. Metal stearate (magnesium stearate) was added to theterpolymer and the terpolymer-copolymer blend. The results are shown inTable 2 below.

Coefficient of restitution (COR) was measured by firing a resulting golfball via an air cannon (at a velocity of 125 feet per second) toward asteel plate positioned 12 feet from the muzzle of the cannon. Therebound velocity was then measured. The rebound velocity was divided bythe velocity of the golf ball leaving the air cannon to give the COR.

The term “compression” as used in the golf ball art generally definesthe overall deflection that a golf ball undergoes when subjected to acompressive load. For example, compression indicates the amount ofchange in a golf ball's shape upon striking. The development of solidcore technology in two-piece or multi-piece solid balls has allowed formuch more precise control of compression in comparison to thread wound,three-piece balls. This result is because in the manufacture of solidcore golf balls, the amount of deflection or deformation is preciselycontrolled by the chemical formula used in making the core(s). Thisdiffers from thread wound, three-piece golf balls in which compressionis controlled in part by the winding process of the elastic thread.Thus, two- and multi-piece (or component) solid core golf balls exhibitmuch more consistent compression readings than balls having thread woundcores (e.g., thread wound three-piece golf balls). In the past, PGAcompression related to a scale of golf ball compression from 0 to 200.The lower the PGA compression value, the softer the feel of the ballupon striking. In practice, tournament quality balls have PGAcompression ratings around 40 to 110, and preferably around 50 to 100.

In determining PGA compression using the 0 to 200 scale, a standardforce is applied to the external surface of the ball. A ball thatexhibits no deflection (0.0 inches of deflection) is rated 200 and aball that deflects 0.2 inches is rated 0. Every change of 0.001 inch indeflection represents a 1 point drop in compression value. Consequently,a ball that deflects 0.1 inches (100 x 0.001 inches) has a PGAcompression value of 100 and a ball that deflects 0.110 inches(110×0.001 inches) has a PGA compression value of 90.

In order to assist in the determination of PGA compression, severaldevices have been employed in the art. For example, PGA compression isdetermined by a golf ball compression tester fashioned in the form of apress with an upper and lower anvil. The upper anvil is at rest againsta 200 pound (lbs) die spring, and the lower anvil is movable through0.300 inches by means of a crank mechanism. In the open position, thegap between the anvils is 1.780 inches, allowing a clearance of 0.200inches for insertion of the ball. As the lower anvil is raised by thecrank mechanism, it compresses the ball against the upper anvil, withsuch compression occurring during the last 0.200 inches of lower anvilstroke. The golf ball then loads the upper anvil, which in turn loadsthe die spring. The equilibrium point of the upper anvil is measured bya dial micrometer. When the upper anvil is deflected by the golf ballmore than 0.100 in (a lesser extent of deflection is simply regarded aszero compression), the reading on the micrometer dial is referred to asthe compression of the ball. In practice, tournament quality golf ballshave PGA compression ratings around 80 to 100, which means that theupper anvil was deflected a total of 0.120 to 0.100 inches. When golfball components (i.e., centers, cores, mantled core, etc.) withdiameters smaller than 1.680 inches are utilized, metallic shims areincluded such that the combined diameter of the shims and the componentis 1.680 inches.

Determining golf ball compression can also be carried out via acompression tester sold by OK Automation, formerly, Atti EngineeringCorporation. This golf ball compression tester is calibrated against acalibration spring provided by OK Automation. The compression valueobtained by such a tester (referred to as Atti compression) relates toan arbitrary value expressed by a number that may range from 0 to 100 (avalue of 200 can also be measured by two revolutions of a dialindicator, which is described below). Atti compression values that areobtained define the deflection that a golf ball undergoes when subjectedto compressive loading. The golf ball compression tester consists of alower movable platform and an upper movable spring-loaded anvil. A dialindicator of the compression tester is mounted such that it measures theupward movement of the spring-loaded anvil. A golf ball to be tested isplaced in the lower platform, which is then raised a fixed distance. Theupper portion of the golf ball comes in contact with and exerts apressure on the spring-loaded anvil, forcing the anvil upward against aspring.

Alternative devices, apparatuses or testers have also been employed todetermine golf ball compression. For example, a modified Riehlecompression device (Riehle Bros. Testing Machine Company) can be used toevaluate the compression of various golf ball components (i.e., cores,mantle cover balls, finished balls, etc.). The modified Riehlecompression device determines golf ball deformation in thousandths of aninch via a load designed to emulate the 200 lbs spring constant of othergolf ball compression testers such as those described above. With amodified Riehle compression device, a Riehle compression value of 61corresponds to a load deflection of 0.061 in. Furthermore, additionalgolf ball compression devices, apparatuses or testers may also beutilized to monitor and evaluate ball compression. Such devices,apparatuses or testers include a Whitney tester and Instron™ device,which can correlate or correspond to, for example, PGA or Atticompression values.

Compression was measured using an Instron™ device, namely, model 5544.Compression of golf ball components were measured based on thedeflection (in inches) caused by a 200 lbs load applied during a loadcontrol mode with a rate of 15 kilopounds per second (kips s⁻¹), anapproach speed of 20 in per minute and a preload of 0.2 pound-force(lbf) (in addition to device system compliance). TABLE 2 #1 #2 #3Escor ™ AT325 (EXY) 100 100 50 Enable ™ 33330 (EY) 0 0 50 % Acrylic Acid6 6 3 % Butyl Acrylate 0 0 16.25 % Methyl Acrylate 20 20 10 %Neutralization 100 100 100 % Mg Stearate 0 28.6 28.6 Compression(Instron) 0.141 0.105 0.118 COR 0.685 0.767 0.705 Nes Factor* 826 872823*Nes factor is determined by taking the sum of the compression and (COR)measurements and multiplying this value by 1,000. The Nes factorrepresents an optimal combination of softer but more resilient golf ballcores.

As can be seen from the results of Example 1 (Table 2), the blend ofsample #3, comprising a blend of the acid terpolymer (EXY) and the alkylacrylate copolymer (EY), produced a sphere with a higher COR than thatcomprising the terpolymer alone (sample #1), while the highlyneutralized terpolymer with the metal stearate had a much higher CORthan the terpolymer without the metal stearate. The addition of themagnesium stearate, as shown above, in both cases increased the COR andthe Nes factor of the sample, producing an enhanced combination ofcompression and resiliency characteristics, as noted by the Nes factorparameter.

Example 2

Additional sample blends of highly neutralized materials with metalstearates were produced and compared against other blends that were nothighly neutralized and had no metal stearates added. The blends weremade up of an olefin/acid copolymer and an olefin/acrylate copolymer.The blends were further neutralized to about 100% in a Banbury™ typemixer using Mg(OH)₂. Zinc stearate was then added to the sample blend,and the blends were extruded into pellets. The sample blends weresubsequently compression molded into neat spheres and tested asdescribed in Example 1. Comparative blends were also produced that werenot further neutralized and did not have metal stearates added (theseblends are labeled “C”). Results are shown in Table 3. TABLE 3 Sample ## 4C # 5C #6C #4 #5 #6 Blend Type Control EX/EY EX/EY Control EX/EYEX/EY Surlyn ™ 100 50 50 100 48.2 48.2 6120 (EX) Lotryl ™ 0 50 50 0 51.851.8 29 MA03 (EY) Fusabond ™ 0 0 5 0 0 0 MG423D % Zn Stearate 0 0 0 33.319 29.5 (approx) % 40 40 40 100 100 100 Neutralization* % Methacrylic 199.5 9 19 9.2 9.2 Acid % Acrylate 0 15 14.5 0 15 15 Compression 0.0490.078 0.098 0.065 0.089 0.090 (Instron) COR 0.742 0.645 0.643 0.7530.697 0.731 Nes Factor 791 723 741 818 786 821*The percent neutralization was estimated based on the metals analysisof the material.

The results in Table 3 show that the COR increases along with the level(amount) of metal stearate or fatty acid salt. Additionally, highlyneutralized thermoplastic material blends of the invention (for example,EX/EY copolymers) that contain metal stearates have a much higher COR(and are considerably softer) than the comparative blends without metalstearates and sample blends that are not as highly neutralized. Sample#6C shows that the addition of a small amount of Fusabond™ produces amuch softer material with the same resiliency or COR.

Example 3

Further examples were produced using different starting materials tocompare an acid copolymer and acid terpolymer (EX/EXY) blend against anacid copolymer and alkyl acrylate copolymer (EX/EY) blend. Threedifferent starting blends were produced as follows: BLEND 1 (EX) BLEND 2(EY) BLEND 3 (EXY) Primacor ™ 5980 Lotryl ™ 29 Escor ™ 100 pbw MA03 100pbw AT325 100 pbw Mg Stearate 66.7 pbw Mg Stearate 67 pbw Mg Stearate66.7 pbw Mg Hydroxide 8.28 pbw Mg Hydroxide 2.43 pbwNote:Primacor ™ 5980 is an ethylene/acrylic acid copolymer (EX) withapproximately 20% acid;Lotryl ™ MA03 is an ethylene/methyl acrylate copolymer (EY) with about29% methyl acrylate; andEscor AT325 is an ethylene/acrylic acid/methyl acrylate terpolymer withabout 6% acid and about 20% methyl acrylate (EXY).

The blends were then mixed together in various combinations andextruded. Neat spheres were produced in the same manner as previouslydiscussed. Results are shown in Table 4 below. TABLE 4 Sample # #7 #8 #9#10 #11 #12 Blend Type EX/ EXY EX/EY EX/EY EX/EY EX/EY EX/EY Blend 1(EX) 25 46.3 46.3 46.3 37.04 37.04 Blend 2 (EY) 0 53.7 45.3 37 53.7 37Blend 3 (EXY) 75 0 0 0 0 0 Primacor ™ 0 0 0 0 5.6 5.6 5980 % Fusabond ™0 0 5 10 0 10 MG-423D % % Acrylic Acid 9.5 9.5 9.5 9.5 9.5 9.5 % Methyl15 15.6 13.1 10.73 15.6 10.73 Acrylate % 100 100 100 100 80 80Neutralization % Mg Stearate 40 40 36.6 40 40 40 Compression 0.091 0.0810.083 0.082 0.082 0.082 (Instron) COR 0.782 0.809 0.797 0.804 0.8050.805 Nes Factor 873 890 880 886 887 887 Shore C/D 82/59 81/59 81/5981/59 81/59 86/60 Breaks/Cracks None 2of 3 2 of 3 1 small 1 of 3 2 of 3crack

The results in Table 4 show that the EX/EY blends have superior COR andNes Factor as compared to the control sample, which is a blend of EX andEXY. The breaks in samples 8 to 12 were the result of molding thespheres at too low of a temperature, thereby forming knit lines thateasily broke.

Example 4

Further examples were produced using different starting materials tocompare an acid copolymer and acid terpolymer blend (EX/EXY) against anacid copolymer and alkyl acrylate copolymer blend (EX/EY). The blendswere mixed (dry blending) together in various combinations and extrudedin a Prism twin screw. Neat spheres were produced in the same manner aspreviously discussed. Results are shown in Table 5 below. TABLE 5 Sample# #13 #14 #15 #16 #17 #18 #19 #20 #21 Blend Type EX/EXY EX/EXY EX/EXYEX/EY EX/EY EX/EY EXY EXY EY Surlyn ™ 9910 (EX) 45 45 45 46 46 46 0 0 0Surlyn ™ 8920 (EX) 30 30 30 39 39 39 0 0 0 Surlyn ™ 8320 (EXY) 25 25 250 0 0 0 0 0 Lotryl ™ 29MA03 0 0 0 15 15 15 0 0 100 (EY) HPF 1000 0 0 0 00 0 100 0 0 HPF 2000 0 0 0 0 0 0 0 100 0 % Mg Stearate 0 40 40 0 4040 * * 0 % Neutralization NA NA ˜90 NA NA ˜90 100 100 0 Comp. (Instron)0.058 0.074 0.078 0.059 0.077 0.080 0.087 0.095 0.257 COR .702 0.7830.803 0.726 0.787 0.797 0.819 0.841 0.528 Nes Factor 760 857 881 785 864877 906 936 785 Shore D 64 60 59 65 59 59 54 51 27

Polymers sold under the trade names HPF™ 1000 and HPF™ 2000 by DuPont,which are commercially available EXY materials presumably produced usinga fatty acids such as magnesium stearate or magnesium oleate, were alsoused in the examples below. Such polymers were used as purchased andwithout modification.

As used herein, the Shore D hardness of a golf ball cover was measuredin accordance with ASTM D-2240, although such measurements were made onthe curved surface of the molded cover rather than on a plaque.Furthermore, the Shore D hardness of golf ball covers were measured withthe cover in place over the core of the ball. When a hardnessmeasurement is made on a dimpled or other aerodynamic patterned cover,Shore D hardness is measured across a land area of the cover.

Sample no. 13 was a control blend of an EX/EXY ionomeric resin. Samplenos. 14 and 15 were blends based on sample no. 13 with magnesiumstearate added at 40% level. Sample no. 15 was additionally neutralizedto about 90%. Sample no. 16 was an unneutralized blend of acidcopolymers and an alkyl acrylate copolymer (EX/EY) without additionalneutralization or fatty acid/fatty acid salt. Samples nos. 17 and 18were blends based on sample no. 16 with magnesium stearate added at 40%level. Sample no.18 was additionally neutralized to about 90%. Samplenos. 19 to 21 consisted of commercially available EXY and EY polymersthat were extruded and molded into neat spheres to show the propertiesof these materials.

The above results clearly show that the addition of fatty acid saltsincreased compression, COR and Nes Factor values of both the controlEX/EXY blends as well as the EX/EY thermoplastic material blends of theinvention. The neutralization of these blends with the fatty acid saltsprovided additional improvement in their properties. Moreover, the EX/EYblends according to the invention are generally softer and faster thanany of the EX/EXY blends known in the art.

Example 5

Further sample blends were produced using different starting materialsto compare an acid copolymer and acid terpolymer blend (EX/EXY) againstan acid copolymer and alkyl acrylate copolymer blend (EX/EY) when eachis used as a cover material on a two-piece golf ball. The blends weremixed (dry blending) together in various combinations and extruded in aPrism twin screw extruder. The golf ball covers were molded over coresto produce a finished two-piece golf ball. The cores used were standardcores (1.557 inches diameter, 37.8 grams, Instrom Compression of 0.107,COR of 0.784, and a Nes Factor of 891). Results are show in Table 6below. Amounts are in parts by weight unless otherwise stated. TABLE 6Sample # #22 #23 #24 #25 #26 #27 #28 #29 Blend Type EX/EXY EX/EXY EX/EXYEX/EY EX/EY EX/EY EXY EXY Surlyn ™ 9910 (EX) 35.5 35.5 35.5 36.5 36.536.5 0 0 Surlyn ™ 8920 (EX) 30 30 30 39 39 39 0 0 Surlyn ™ 8320 25 25 250 0 0 0 0 (EXY) Lotryl ™ 29MA03 0 0 0 15 15 15 0 0 (EY) HPF 1000 (EXY) 00 0 0 0 0 97.5 0 HPF 2000 (EXY) 0 0 0 0 0 0 0 97.5 Mg Stearate 0 0 66.70 66.7 0 * * Ca Stearate 0 66.7 0 0 0 66.7 0 0 Masterbatch 9.5 9.5 9.59.5 9.5 9.5 0 0 TiO₂ 0 1.6 1.6 0 1.6 1.6 2.5 2.5 Comp. (Instron) 0.1000.099 0.102 0.100 0.100 0.099 0.105 0.105 COR 0.793 0.804 0.796 0.7930.796 Broke 0.796 0.790 Nes Factor 893.6 902.7 897.2 893.6 895.7 NA901.2 894.6 Shore D 65 67 63-64 65 62-63 66-67 60 54-55*HPF 1000 and HPF 2000 are commercially available EXY materialspresumably produced using a fatty acid, such as magnesium stearate ormagnesium oleate. The HPF materials were used as purchased.

Sample no. 22 was a control sample of a prior art EX/EXY blend. Sampleno. 25 was a control sample blend of EX/EY with no fatty acid salt addedto the blend. As shown in the above results, sample blends of bothEX/EXY and EX/EY that are modified with both magnesium stearate andcalcium stearate have increased COR and Nes Factor values as compared tosamples that are not modified with a fatty acid. Magnesium stearate canlower the Shore D hardness value, while calcium stearate generallyincreases the Shore D hardness value. Therefore, depending on thedesired final properties of a golf ball cover (or mantle), differentfatty acids may be used.

In one embodiment, a golf ball 10 is constructed with a cover 16composed of a polyurethane material as set forth in U.S. Pat. No.6,117,024 from which pertinent parts are hereby incorporated byreference. The golf ball 10 has a core 12, a boundary layer 14 or bothcomposed of a thermoplastic material of the present invention. The golfball 10 preferably has a COR at 143 feet per second greater than 0.7964and a USGA initial velocity less than 255.0 feet per second. The golfball 10, more preferably, has a COR of approximately 0.8152 at 143 feetper second, and an initial velocity between 250 to 255 feet per secondunder USGA initial velocity conditions. A more thorough description of ahigh COR golf ball is disclosed in U.S. Pat. No. 6,443,858 from whichpertinent parts are hereby incorporated by reference.

Additionally, the core of a golf ball 10 may be solid, hollow or filledwith a fluid such as a gas or liquid. The golf ball can also have ametal mantle. The cover 16 of the golf ball 10 maybe any suitablematerial. A preferred cover for a three-piece golf ball is composed of athermoset polyurethane material. Alternatively, the cover 16 is composedof a thermoplastic polyurethane, ionomeric resin blend, ionomeric rubberblend, ionomeric resin, thermoplastic polyurethane blend or like.Alternatively, the golf ball 10 may have a thread layer. Those skilledin the pertinent art will recognize that other cover materials may beutilized without departing from the scope and spirit of the presentinvention. The golf ball 10 may have a finish of one or two base-coatsand/or one or two top-coats.

In an alternative embodiment of a golf ball 10, the boundary layer 14 orcover layer 16 is comprised of a high acid (i.e., greater than 16 weight% acid) ionomeric resin or high acid ionomeric resin blend and the core12 is composed of a thermoplastic material of the present invention.Alternatively, if the cover layer 16 is composed of a high acidionomeric resin or a high acid ionomeric resin blend, then the boundarylayer 14 and/or core 12 is composed of the thermoplastic material of thepresent invention. More preferably, the boundary layer 14 is comprisedof a blend of two or more high acid (i.e., greater than 16 weight %acid) ionomeric resins neutralized, to various extents, by differentmetal cations.

In an alternative embodiment of a golf ball 10, the boundary layer 14 orcover layer 16 is comprised of a low acid (i.e., 16 weight % acid orless) ionomeric resin or low acid ionomeric resin blend. Preferably, theboundary layer 14 is comprised of a blend of two or more low acid (i.e.,16 weight % acid or less) ionomeric resins neutralized, to variousextents, by different metal cations. The boundary layer 14 compositionsof the embodiments described herein may include high acid ionomericresins such as those developed by DuPont under the trade name Surlyn™,and by ExxonMobil under the Escor™ or Iotek™ trade names or blendsthereof. Examples of compositions that maybe used as the boundary layer16 herein are set forth in detail in U.S. Pat. No. 5,688,869, which isincorporated herein by reference. Of course, such high acid ionomericresin compositions are not limited in any way by those compositions setforth in U.S. Pat. No. 5,688,869. The compositions set forth in U.S.Pat. No. 5,688,869 are incorporated herein byway of example only.

High acid ionomeric resins that may be suitable for use in formulatingthe boundary layer 14 compositions are copolymers that are the metal(such as sodium, zinc, magnesium, etc.) salts of the reaction product ofan olefin having from about 2 to 8 carbon atoms and an unsaturatedmonocarboxylic acid having from about 3 to 8 carbon atoms. Preferably,the ionomeric resins are copolymers of ethylene and either acrylic ormethacrylic acid. In some circumstances, an additional comonomer such asan acrylate ester (for example, iso- or n-butylacrylate, etc.) can alsobe included to produce a softer terpolymer. The carboxylic acid groupsof the acid copolymer are partially neutralized (for example,approximately 10 to 100%, preferably, 30 to 70%) by the metal cations.Each of the high acid ionomeric resins that may be included in the innerlayer components of a golf ball (components, for example, composed inpart of a thermoplastic material of the invention) contains greater than16% by weight of a carboxylic acid, preferably from about 17 to about25% by weight of a carboxylic acid and, more preferably from about 18.5to about 21.5% by weight of a carboxylic acid. Examples of high acidmethacrylic acid ionomeric resins found suitable for use in accordancewith the present invention include, but are not limited to, Surlyn™ 8220and 8240 (both formerly known as forms of Surlyn™ AD-8422), Surlyn™ 9220(zinc cation), Surlyn™ SEP-503-1 (zinc cation) and Surlyn™SEP-503-2(magnesium cation). According to DuPont, all of these ionomeric resinscontain from about 18.5 to about 21.5% by weight methacrylic acid.Examples of high acid acrylic acid ionomeric resins suitable for use inthe present invention also include, but are not limited to, the highacid ethylene/acrylic acid copolymers produced by ExxonMobil such as Ex™1001, 1002, 959,960, 989, 990,1003, 1004, 993 and 994. Moreover, Escor™or Iotek™ 959 are also copolymers that can be used with the presentinvention. According to ExxonMobil, Iotek™ 959 and 960 contain fromabout 19.0 to about 21.0% byweight acrylic acid with approximately 30 toabout 70% of the acid groups neutralized with sodium and zinc cations,respectively.

Furthermore, a number of high acid ionomeric resins or ionomeric resinblends neutralized, to various extents, by several different types ofmetal cations such as manganese, lithium, potassium, calcium, sodium,zinc, magnesium and nickel cations are also available for use in golfball component production as described herein. It has also been foundthat manganese, lithium, potassium, calcium or nickel metal cations canneutralize high acid ionomeric resin blends to produce boundary layer 16compositions exhibiting enhanced hardness and resiliency due tosynergies that occur during production. Consequently, high acidionomeric resins and ionomeric resin blends neutralized with manganese,lithium, potassium, calcium or nickel cations can be blended to producesubstantially higher CORs than those yielded by low acid ionomeric resinboundary layer 16 compositions that are commercially available.

More particularly, several high acid ionomeric resins have been producedby using a variety of metal cation salts to neutralize, to variousextents, polymers comprising an alpha olefin and an alpha,beta-unsaturated carboxylic acid such as disclosed by U.S. Pat. No.5,688,869, which has been incorporated herein by reference. It has alsobeen found that numerous metal cation neutralized, high acid ionomericresins can be obtained by reacting a high acid polymer (i.e., a polymercontaining greater than 16% by weight acid, preferably, from about 17 toabout 25% by weight acid and, more preferably, about 20% by weightpercent acid) with a metal cation salt capable of ionizing orneutralizing the polymer to a desired extent (for example, from about 10to 90%).

Such a copolymer can be made up of greater than 16% by weight of analpha, beta-unsaturated carboxylic acid and an alpha olefin. Optionally,a softening comonomer can be included in the copolymer. Generally, thealpha olefin has from 2 to 10 carbon atoms and, preferably, is ethylene.Preferably, the unsaturated carboxylic acid is a carboxylic acid havingfrom about 3 to 8 carbon atoms. Examples of such acids include acrylicacid, methacrylic acid, ethacrylic acid, chloroacrylic acid, crotonicacid, maleic acid, fumaric acid and itaconic acid with acrylic acidbeing preferred.

A softening comonomer can be optionally included in the boundary layer14 of a golf ball as described herein. The softening comonomer can beselected from the group consisting of vinyl esters of aliphaticcarboxylic acids having 2 to 10 carbon atoms, vinyl ethers having alkylgroups that contain 1 to 10 carbon atoms and alkyl acrylates ormethacrylates in which the alkyl group contains 1 to 10 carbon atoms.Suitable softening comonomers include vinyl acetate, methyl acrylate,methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate,butyl methacrylate or the like.

Examples of a number of copolymers suitable for use in a thermoplasticmaterial of the present invention include, but are not limited to, highacid embodiments of an ethylene/acrylic acid copolymer, anethylene/methacrylic acid copolymer, an ethylene/itaconic acidcopolymer, an ethylene/maleic acid copolymer, anethylene/methacrylicacid/vinyl acetate terpolymer, an ethylene/acrylic acid/vinyl alcoholterpolymer, etc. The base copolymer broadly contains greater than 16% byweight unsaturated carboxylic acid, from about 39 to about 83% by weightethylene and from 0 to about 40% by weight of a softening comonomer.Preferably, the copolymer contains about 20% byweight unsaturatedcarboxylic acid and about 80% byweight ethylene. Mostpreferably, thecopolymer contains about 20% acrylic acid with the remainder beingethylene.

Boundary layer 14 compositions may also include low acid ionomericresins such as those developed and sold by DuPont under the trade nameSuryln™ and ExxonMobil under the trade names Escor™ and Iotek™ as wellas any blends thereof.

Another embodiment of a boundary layer 14 of a golf ball can comprisenon-ionomeric thermoplastic material or thermoset materials. Suitablenon-ionomeric materials include, but are not limited to,metallocene-catalyzed polyolefins or polyamides, metallocene-catalyzedpolyamide/ionomeric resin blends, polyphenylene ether/ionomeric resinblends, etc., which preferably have a Shore D hardness of at least 60(or a Shore C hardness of at least about 90) and a flex modulus ofgreater than about 30,000 psi, preferably, greater than about 50,000psi, or other hardness and flex modulus values that are comparable tothe properties of the ionomeric resins described above. Other suitablematerials include, but are not limited to, thermoplastic orthermosetting polyurethanes, thermoplastic block polyesters (forexample, a polyester elastomer such as that sold by DuPont under thetrade name Hytrel™), or thermoplastic block polyamides (for example, apolyether amide such as that sold by Elf Atochem S.A. under the tradename Pebex™, a blend of two or more non-ionomeric thermoplasticelastomers, or a blend of one or more ionomeric resins and one or morenon-ionomeric thermoplastic elastomers. Such materials can be blendedwith the ionomeric resins described above in order to reduce overallgolf ball manufacturing costs.

Additional materials suitable for use in the boundary layer 14 or coverlayer 16 of a golf ball as set forth herein include polyurethanes, whichare described in more detail below.

In one embodiment, the cover layer 16 is comprised of a relatively soft,low flex modulus (about 500 to about 50,000 psi, preferably about 1,000to about 25,000 psi, and more preferably about 5,000 to about 20,000psi) material or blend of materials. Preferably, the cover layer 16comprises a polyurethane, a polyurea, a blend of two or morepolyurethanes/polyureas or a blend of one or more ionomeric resins ornon-ionomeric thermoplastic materials with a polyurethane/polyurea. Morepreferably, the cover layer comprises a thermoplastic polyurethane or areaction injection molded polyurethane/polyurea as described in moredetail below.

The cover layer 16 preferably has a thickness in the range of 0.005 toabout 0.15 inch, more preferably about 0.010 to about 0.050 inch andmost preferably 0.015 to 0.025 inch. In one embodiment, the cover layer14 has a Shore D hardness of 60 or less (or a Shore C hardness less than90) and more preferably 55 or less (or a Shore C hardness of about 80 orless). In another preferred embodiment, the cover layer 16 iscomparatively harder than the boundary layer 14.

In one preferred embodiment, the cover layer 16 comprises apolyurethane, a polyurea or a blend of polyurethanes/polyureas.Polyurethanes are polymers that are used to form a broad range ofproducts. These polymers are generally formed by mixing two primaryingredients during processing. For the most commonly used polyurethanes,the two primary ingredients are a polyisocyanate (for example,4,4′-diphenylmethane diisocyanate monomer, MDI, toluene diisocyanate,TDI, or derivatives thereof) and a polyol (for example, a polyesterpolyol or a polyether polyol).

A wide range of combinations of polyisocyanates and polyols (as well asother ingredients) are available for yielding polyurethanes such asdescribed above. Furthermore, the properties of polyurethanes can becontrolled by the types of ingredients used. For example, a polyurethanecan be a thermoset type (a cross-linked molecular structure that isgenerally not flowable with heat) or thermoplastic type (a linearmolecular structure that is generally flowable with heat).

Cross-linking of a thermoset polyurethane can occur between isocyanategroups (NCO) and the hydroxyl end-groups of polyols. Cross-linking willalso occur between NH₂ groups of the amines and NCO groups of theisocyanates to form a polyurea. Additionally, the characteristics ofsuch polyurethanes as described above can also be controlled bydifferent types of reactive chemicals and processing parameters. Forexample, catalysts can be used to control polymerization rates.Depending on the processing method employed, polymerization rates can bevery quick (as in the case for some reaction injection molding, RIM,systems) or may be on the order of several hours (as in several coatingsystems such as a cast system). Consequently, a great variety ofpolyurethanes are suitable for different end-uses.

Polyurethanes are typically classified as thermosetting or thermoplasticmaterials. A polyurethane becomes irreversibly “set” when a polyurethaneprepolymer is cross-linked with a polyfunctional curing agent such as apolyamine or a polyol. The prepolymer typically is made from polyetheror polyester. A prepolymer is typically an isocyanate-terminated polymerthat is produced by reacting an isocyanate with a moiety that has activehydrogen groups such as a polyester and/or polyether polyol. Forexample, the moiety can be a hydroxyl group. Diisocyanate polyethers arethe preferred polyurethanes set forth herein because of their waterresistance.

The physical properties of thermoset polyurethanes are controlledsubstantially by the degree of cross-linking and by the content of hardand soft segments. Tightly cross-linked polyurethanes are fairly rigidand strong. A lower amount of cross-linking results in materials thatare flexible and resilient. Thermoplastic polyurethanes have somecross-linking, although such cross-linking is primarily by physicalmeans, for example, hydrogen bonding. Cross-linking bonds of athermoplastic polyurethane can be reversibly broken by increasingtemperatures such as during molding or extrusion. In this regard,thermoplastic polyurethanes can be injection molded and extruded as asheet or blow film. Thermoplastic polyurethanes can be used up to about400° F. and are available in a wide range of hardnesses.

Polyurethane materials suitable for use with the present invention maybe formed by the reaction of a polyisocyanate, a polyol and, optionally,one or more polymer chain extenders. The polyol component can includeany suitable polyether or polyester polyol. Additionally, in analternative embodiment, the polyol component is polybutadiene diol. Thepolymer chain extenders include, but are not limited to, diols, triolsand amine extenders. Any suitable polyisocyanate may be used to form apolyurethane as set forth herein. The polyisocyanate is preferablyselected from the group of diisocyanates including, but not limited to,MDI, 2,4-TDI, m-xylylene diisocyanate (XDI), methylene bis-(4-cyclohexylisocyanate) (HMDI), hexamethylene diisocyanate (HDI),naphthalene-1,5,-diisocyanate (NDI), 3,3′-dimethyl-4,4′-biphenyldiisocyanate (TODI), 1,4-diisocyanate benzene (PPDI),phenylene-1,4-diisocyanate and 2,2,4- or 2,4,4-trimethyl hexamethylenediisocyanate (TMDI). Other less preferred diisocyanates include, but arenot limited to, isophorone diisocyanate (IPDI), 1,4-cyclohexyldiisocyanate (CHDI), diphenylether-4,4′-diisocyanate, p,p′-diphenyldiisocyanate, lysine diisocyanate (LDI), 1,3-bis (isocyanato methyl)cyclohexane and polymethylene polyphenyl isocyanate (PMDI).

One additional polyurethane component that can also be used incorporatesmeta-tetramethylxylylene diisocyanate (TMXDI) aliphatic isocyanate.Polyurethanes based on TMXDI aliphatic isocyanate can provide improvedgloss retention UV light stability, thermal stability and hydrolyticstability. Additionally, TMXDI aliphatic isocyanate has demonstratedfavorable toxicological properties. Furthermore, given that TMXDIaliphatic isocyanate has a low viscosity, it is usable with a widerrange of diols (to polyurethane) and diamines (to polyareas). If TMXDIaliphatic isocyanate is used, it typically (although not necessarily)can be added as a direct replacement for some or all of the otheraliphatic isocyanates. Because of the slow reactivity of TMXDI aliphaticisocyanate, it may be useful or necessary to use catalysts in order toachieve practical demolding times. Hardness, tensile strength andelongation can be adjusted by adding further materials to such apolyurethane component.

For a soft cover layer 16 preferably comprises a polyurethane with aShore D hardness of from about 10 to about 55 (a Shore C hardness ofabout 15 to about 75), more preferably, from about 25 to about 55 (aShore C hardness of about 40 to about 75) and, most preferably, fromabout 30 to about 55 (a Shore C hardness of about 45 to about 75).Alternatively, for a hard cover layer 16 a Shore D hardness should befrom about 20 to about 90, preferably, from about 30 to about 80 and,more preferably, from about 40 to about 70.

The polyurethane material preferably has a flex modulus from about 1 toabout 310 Kpsi, more preferably, from about 3 to about 100 Kpsi and mostpreferably from about 3 to about 40 Kpsi for a soft cover layer.Alternatively, for a hard cover layer 14 the flex modulus should beabout 40 to 90 Kpsi.

Non-limiting examples of a polyurethane suitable for use in the coverlayer 16 (or boundary layer 14) include a thermoplastic polyesterpolyurethane such as sold by Bayer Corporation under the trade nameTexin™ (for example, Texin™ DP7-1097 and Texin™ 285) and by B.F.Goodrich under the trade name Estane™ (for example, Estane™ X-4517). Thethermoplastic polyurethane material may be blended with a soft ionomericresin or other non-ionomer. For example, polyamides blend well with softionomeric resins.

Other soft, relatively low modulus non-ionomeric thermoplastic orthermoset polyurethane materials may also be utilized so as long as thematerials can produce the desired playability and durabilitycharacteristics. These materials include, but are not limited to,thermoplastic polyurethanes such as Pellethane™ as sold by Dow ChemicalCompany and non-ionomeric thermoset polyurethanes such as disclosed inU.S. Pat. No. 5,334,673, which is incorporated herein by reference.

Typically, there are two classes of thermoplastic polyurethanematerials, namely, aliphatic polyurethanes and aromatic polyurethanes.Aliphatic polyurethanes are produced from a polyol or polyols andaliphatic isocyanates such as H₁₂MDI or HDI. Aromatic polyurethanes areproduced from a polyol or polyols and aromatic isocyanates such as MDIor TDI. Thermoplastic polyurethane materials may also be produced from ablend of both aliphatic and aromatic polyurethanes such as a blend ofHDI and TDI with a polyol or polyols.

Generally, aliphatic thermoplastic polyurethanes are lightfast meaningthat they do not yellow appreciably upon exposure to ultraviolet (UV)light. Conversely, aromatic thermoplastic polyurethanes tend to yellowupon exposure to UV light. One method of stopping the yellowing ofaromatic polyurethanes is to paint the outer surface of a finished golfball comprising such a polyurethane with a coating containing a pigment,such as titanium dioxide,so that the UV light is prevented from reachingthe surface of the ball. Another method is to add UV absorbers, opticalbrighteners and stabilizers to a clear coating(s) on the outer cover ofthe golf ball as well as to the thermoplastic polyurethane materialitself. By adding UV absorbers and stabilizers to the thermoplasticpolyurethane and the golf ball coatings, aromatic polyurethanes can beeffectively used in the outer cover layer of a ball. This result isadvantageous as aromatic polyurethanes typically have better scuffresistance characteristics and cost less than aliphatic polyurethanes.

Other suitable polyurethane materials for use golf balls as set forthherein include reaction injection molded (“RIM”) polyurethanes. RIM is aprocess by which highly reactive liquids are injected into a mold andmixed (usually by impingement and/or mechanical mixing in an in-linedevice such as a “peanut mixer”). The reactive liquids polymerizeprimarily in the mold to form a coherent, one-piece molded article. ARIM process usually involves a rapid polymerization reaction between oneor more reactive components (such as a polyether or polyester polyol,polyamine or other material with an active hydrogen) and one or moreisocyanate containing constituents. Often the reaction occurs in thepresence of a catalyst. The reactive liquids are stored in separatetanks prior to molding and may be first mixed in a mix head, which isupstream of the mold. After mixing, the liquids can be injected into themold. The liquid streams are metered in a desired weight-to-weight ratioand fed into an impingement mix head, with mixing occurring under highpressure, for example, 1,500 to 3,000 psi. The liquid streams impingeupon each other in the mixing chamber of the mix head and the resultingmixture is injected into the mold. One of the liquid streams typicallycontains a catalyst for the polymerization reaction. The constituentliquids react rapidly after mixing to gel and form polyurethanepolymers. Polyureas, epoxies and various unsaturated polyesters also canbe molded by RIM processes. Further descriptions of suitable RIM systemsare disclosed in U.S. Pat. No. 6,663,508 from which pertinent parts arehereby incorporated by reference.

Non-limiting examples of suitable RIM materials for use as set forthherein are Bayflex™, Baydur™ GS and Prism™ materials sold by BayerCorporation. Spectrim™ RIM materials from Dow Chemical Company includingSpectrim™ MM 373-A (isocyanate) and 373-B (polyol) can also be used. Inaddition, Elastolit™ SR RIM materials from BASF Corporation can also beused. Preferred RIM materials include Bayflex™ MP-10000, MP-7500 and110-50 (filled or unfilled). Further preferred examples are polyols,polyamines and isocyanates formed by processes that recyclepolyurethanes and polyureas. Additionally, such processes may bemodified by incorporating a butadiene component in a diol agent.

Another preferred embodiment is a golf ball in which at least one of theboundary layer 14 and/or the cover layer 16 comprise afast-chemical-reaction-produced component. This component comprises atleast one material selected from the group consisting of polyurethane,polyurea, polyurethane ionomeric resin, epoxy, and unsaturatedpolyesters, and preferably comprises polyurethane, polyurea or a blendcomprising polyurethanes and/or other polymers. A particularly preferredform of the invention is a golf ball with a cover comprisingpolyurethane or a polyarethane blend.

Polyol components typically contain additives such as stabilizers, flowmodifiers, catalysts, combustion modifiers, blowing agents, fillers,pigments, optical brighteners and release agents to modify physicalcharacteristics of the golf ball cover. Also, polyurethane/polyureaconstituent molecules derived from recycled polyurethane can be added tothe polyol component.

The surface geometry of a golf ball 10 is preferably a conventionaldimple pattern such as disclosed in U.S. Pat. No. 6,213,898 from whichpertinent parts are hereby incorporated by reference. Alternatively, thesurface geometry of the golf ball 10 may have a non-dimple pattern suchas disclosed in U.S. Pat. No. 6,290,615 from which pertinent parts arehereby incorporated by reference.

From the foregoing it is believed that those skilled in the pertinentart will recognize the meritorious advancement of this invention andwill readily understand that while the present invention has beendescribed in association with a preferred embodiment thereof and otherembodiments illustrated in the accompanying drawings, numerous changes,modifications and substitutions of equivalents may be made thereinwithout departing from the spirit and scope of this invention, which isintended to be unlimited by the foregoing except as may appear in thefollowing appended claims. Therefore, the embodiments of the inventionin which an exclusive property or privilege is claimed are defined inthe following appended claims.

1. A thermoplastic material comprising: a first copolymer comprising analpha olefin and an alpha, beta-unsaturated carboxylic acid; a secondcopolymer of an alpha olefin and an alkyl acrylate; and a fatty acid orsalt of a fatty acid; wherein the thermoplastic material is partially tohighly neutralized.
 2. The thermoplastic material according to claim 1,wherein the alpha olefin is ethylene.
 3. The thermoplastic materialaccording to claim 1, wherein the thermoplastic material is from about10 to about 100 percent neutralized.
 4. The thermoplastic materialaccording to claim 1, wherein the fatty acid or fatty acid saltcomprises from about 10 to about 60 parts by weight of thermoplasticmaterial.
 5. The thermoplastic material according to claim 1, whereinthe fatty acid salt is a metal stearate.
 6. The thermoplastic materialaccording to claim 5, wherein the metal stearate is selected from thegroup consisting of calcium stearate, magnesium stearate, zinc stearate,barium stearate, aluminum stearate, lithium stearate and sodiumstearate.
 7. The thermoplastic material according to claim 1, furthercomprising a second fatty acid or fatty acid salt.
 8. A thermoplasticmaterial comprising: a first copolymer comprising an alpha olefin and analpha, beta-unsaturated carboxylic acid, a second copolymer of anethylene and an alkyl acrylate, and a fatty acid or salt of a fattyacid, wherein the thermoplastic material is neutralized from 50% to100%.
 9. The thermoplastic material according to claim 8, wherein theblend comprises from about 10 to about 60 parts by weight fatty acid orfatty acid salt.
 10. The thermoplastic material according to claim 8,wherein the fatty acid salt is a metal stearate.
 11. The thermoplasticmaterial according to claim 10, wherein the metal stearate is selectedfrom the group consisting of calcium stearate, magnesium stearate, zincstearate, barium stearate, aluminum stearate, lithium stearate andsodium stearate.
 12. A thermoplastic material comprising: a firstcopolymer comprising an alpha olefin, an alpha, beta-unsaturatedcarboxylic acid and a softening comonomer; a second copolymer of analpha olefin and an alkyl acrylate; and a fatty acid or salt of a fattyacid; wherein the thermoplastic material is partially to highlyneutralized.